College of Animal Science and Veterinary Medicine, Jilin University, Changchun, PR China.
Virol J. 2010 Sep 24;7:254. doi: 10.1186/1743-422X-7-254.
The spike proteins of coronaviruses associate with cellular molecules to mediate infection of their target cells. The characterization of cellular proteins required for virus infection is essential for understanding viral life cycles and may provide cellular targets for antiviral therapies.
We identified Neural Cell Adhesion Molecule (NCAM) as a novel interacting partner of the PHE-CoV S protein. A T7 phage display cDNA library from N2a cells was constructed, and the library was screened with the soluble PHE-CoV S glycoproteins. We used a coimmunoprecipitation assay to show that only the NCAM was a binding partner of spike protein. We found that a soluble form of anti-NCAM antibody blocked association of the PHE-CoV with N2a cells. Furthermore, double-stranded siRNA targeted against NCAM inhibited PHE-CoV infection.
A novel interaction was identified between NCAM and spike protein and this association is critical during PHE-CoV infection.
冠状病毒的刺突蛋白与细胞分子结合,介导其靶细胞的感染。鉴定病毒感染所需的细胞蛋白对于理解病毒生命周期至关重要,并且可能为抗病毒治疗提供细胞靶标。
我们鉴定出神经细胞黏附分子(NCAM)是 PHE-CoV S 蛋白的一种新的相互作用伙伴。用 T7 噬菌体展示 cDNA 文库从 N2a 细胞构建文库,并使用可溶性 PHE-CoV S 糖蛋白筛选文库。我们使用共免疫沉淀测定表明只有 NCAM 是 Spike 蛋白的结合伙伴。我们发现一种可溶性抗 NCAM 抗体可阻断 PHE-CoV 与 N2a 细胞的结合。此外,针对 NCAM 的双链 siRNA 抑制了 PHE-CoV 的感染。
鉴定到 NCAM 与 Spike 蛋白之间存在新的相互作用,这种关联在 PHE-CoV 感染过程中至关重要。